TS 7000Recalls & reported problems across all models

We found 3 models of TS 7000 by Baxter Medical Systems GmbH + Co. KG in the FDA's device registry (GUDID). Together they are named in 26 adverse event reports in the FDA's MAUDE database, received between May 8, 2023 and Sep 25, 2026 — classified as 1 injury, 25 malfunctions.

The most frequently reported specific device problem is “Unintended Movement” (9 reports).

1 FDA recall record name at least one of these models by its device identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

TS 7000 recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

1. Sep 19, 2024Open, Classified

   The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.

   Z-0210-2025 · Root cause: Device Design · names 3 of these models · Recall details · FDA record ↗

Most reported TS 7000 problems

TS 7000 models

3 models, most reported first. Each model has its own page with its reports, recalls and device details.

• TS 7000 1723633

  TABLE, OPERATING-ROOM, ELECTRICAL
  1 recall22 reports
• TS 7000 1604788

  TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, AC-POWERED
  1 recall4 reports
• TS 7000 1604786

  Table, radiologic
  1 recall0 reports

Recent TS 7000 adverse event reports

The 15 most recent reports across all models, in the reporter's own words as published by the FDA.

• MalfunctionSep 25, 2026Unintended Movement

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50900045 ↗
• MalfunctionSep 10, 2026Unintended System Motion

  Baxter received a report that Operating table TruSystem 7000 U (dV) had table will move without any control button press. The process step during which this occurred was unknown. There was no patient/user injury, medical intervention, symptom, or adverse event reported.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50703689 ↗
• MalfunctionApr 14, 2026Unintended Movement; Device Fell

  BAXTER RECEIVED A REPORT THAT OPERATING TABLE TRUSYSTEM 7000 HAD AN UNINTENDED MOVEMENT WHEN RAISING THE TABLE. IT WAS NOTED WHEN RESETTING THE TABLE, IT DROPPED TO THE FLOOR. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24872612 ↗
• MalfunctionApr 10, 2026Unstable

  BAXTER RECEIVED A REPORT THAT OR TABLE TRUSYSTEM 7000 U HAD WOBBLE MOVEMENT WHEN BRAKES ENGAGE. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24840651 ↗
• MalfunctionMar 11, 2026Key or Button Unresponsive/not Working

  BAXTER RECEIVED A REPORT STATING THAT OPERATING TABLE TRUSYSTEM 7000 WAS WOBBLY. THERE WAS NO INJURY, DEATH, OR PROCEDURAL DELAY REPORTED WITH THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24568115 ↗
• MalfunctionMar 11, 2026Key or Button Unresponsive/not Working

  BAXTER RECEIVED A REPORT STATING THAT DURING SURGICAL PROCEDURE, OR TABLE TRUSYSTEM 7000 U (DV) WAS UNABLE TO BE ACTIVATING. NO OPERATION WAS POSSIBLE FROM THE REMOTE CONTROL AND THE COLUMN KEYPAD. USER TRIED EMERGENCY OVERRIDE AND POWERED OFF TABLE SEVERAL TIMES WITH NO CHANGE. THERE WAS NO INJURY, DEATH, OR PROCEDURAL DELAY REPORTED WITH THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24568061 ↗
• MalfunctionMar 10, 2026Key or Button Unresponsive/not Working

  BAXTER RECEIVED A REPORT STATING THAT OPERATING TABLE TRUSYSTEM 7000 WAS NOT PROVIDING ANY FUNCTION WHILE ACTIVATING. THE BED WAS LOCATED AT THE ACCOUNT. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24561332 ↗
• MalfunctionMar 6, 2026Positioning Failure; Key or Button Unresponsive/not Working

  BAXTER RECEIVED A REPORT STATING THAT OR TABLE TRUSYSTEM 7000 U (DV) WAS STUCK IN TRENDLEBURG AND NO FUNCTION WAS POSSIBLE TO ACTIVATE. CUSTOMER TRIED RESETTING TABLE BUT THIS DID NOT RESOLVE THE ISSUE. THERE WAS NO INJURY, DEATH, OR PROCEDURAL DELAY REPORTED WITH THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24536036 ↗
• MalfunctionFeb 3, 2026Positioning Failure; Mechanical Problem

  BAXTER RECEIVED A REPORT STATING THAT DURING A PROCEDURE, A OPERATING TABLE TRUSYSTEM 7000 WAS STUCK IN TREND MODE AND WAS UNABLE TO MOVE THE TABLE. REMOTE SCREEN IS BLACK AND ON BUTTON IS FLASHING. THE PATIENT WAS UNINJURED, AND THE PROCEDURE WAS FINISHED WITHOUT INCIDENT. NO HARM OR SIGNIFICANT IMPACT TO THE SURGICAL PROCEDURE WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24248028 ↗
• MalfunctionDec 1, 2025Unintended Movement; Unintended Movement

  BAXTER RECEIVED A REPORT STATING THAT OPERATING TABLE TRUSYSTEM 7000 MOVED WITH THE FLOOR LOCKS ON AND WITHOUT REMOTE GUIDANCE. NO HARM OR SIGNIFICANT IMPACT TO THE SURGICAL PROCEDURE WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23681406 ↗
• MalfunctionNov 25, 2025Mechanical Jam; Key or Button Unresponsive/not Working; Mechanical Jam; Key or Button Unresponsive/not Working

  BAXTER RECEIVED A REPORT STATING THAT DURING A CASE, THE TRUSYSTEM 7000 TABLE WAS MOVING UP, THE TABLE MADE A LOUD SOUND AND NO FUNCTIONS WERE AVAILALE AFTER THAT. NO HARM OR SIGNIFICANT IMPACT TO THE SURGICAL PROCEDURE WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23645758 ↗
• MalfunctionNov 18, 2025Unintended Movement; Device Fell; Unintended Movement; Device Fell

  BAXTER RECEIVED A REPORT STATING THAT OPERATING TABLE TRUSYSTEM 7000 (PRODUCT CODE 1723633, SERIAL NUMBER (B)(6)), WAS IN REVERSE TRENDELENBURG POSITION, THE TABLE SLID DOWNWARD AND THE FOOT END OF THE TABLE ¿CRUSHED A NURSE¿S FOOT¿. THE NURSE WAS SEEN IN THE EMERGENCY DEPARTMENT, AND IT WAS REPORTED THE NURSE HAD A BRUISED FOOT.

  Patient problems: Bruise/Contusion

  MAUDE report 23585966 ↗
• MalfunctionNov 12, 2025Unintended Movement; Unintended Movement

  BAXTER RECEIVED A REPORT STATING THAT OR TABLE TRU SYSTEM 7000 U HEAD SECTION WILL NOT STAY IN PLACE. NO HARM OR SIGNIFICANT IMPACT TO THE SURGICAL PROCEDURE WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23538689 ↗
• MalfunctionAug 26, 2025Sparking; Material Split, Cut or Torn; Sparking; Material Split, Cut or Torn

  BAXTER RECEIVED A REPORT STATING THAT OPERATING TABLE TRUSYSTEM 7000 PLUG-IN PORT WAS RIPPED AND COMPLETELY UNHOUSED, GENERATING SOME SPARKS WHEN PLUGGED IN. THERE WAS NO PATIENT/USER INJURY, MEDICAL INTERVENTION, SYMPTOM, OR ADVERSE EVENT REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22896528 ↗
• MalfunctionAug 21, 2025Unintended Movement; Unintended Movement

  BAXTER RECEIVED A REPORT STATING THAT OPERATING TABLE TRUSYSTEM 7000 WAS UNLOCKING IN THE MIDDLE OF THE PROCEDURE. NO HARM OR SIGNIFICANT IMPACT TO THE SURGICAL PROCEDURE WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22862537 ↗

Other Baxter Medical Systems GmbH + Co. KG products

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• TL 5000/3000 – Surgical Light2 models · 2 reports · 1 recall
• VidiaPort3 models · 1 reports · 1 recall
• iLED5 models · 41 reports